{"id":2653,"date":"2026-02-28T13:00:43","date_gmt":"2026-02-28T13:00:43","guid":{"rendered":"https:\/\/www.bestheartsurgery.com\/blog\/inotropic-agents-definition-clinical-significance-and-overview\/"},"modified":"2026-02-28T13:00:43","modified_gmt":"2026-02-28T13:00:43","slug":"inotropic-agents-definition-clinical-significance-and-overview","status":"publish","type":"post","link":"https:\/\/www.bestheartsurgery.com\/blog\/inotropic-agents-definition-clinical-significance-and-overview\/","title":{"rendered":"Inotropic Agents: Definition, Clinical Significance, and Overview"},"content":{"rendered":"\n<h2 class=\"wp-block-heading\">Inotropic Agents Introduction (What it is)<\/h2>\n\n\n\n<p>Inotropic Agents are medications that change the force of heart muscle contraction.<br\/>\nThey are a therapy used in cardiovascular and critical care medicine.<br\/>\nThey are most often used when cardiac output is inadequate for the body\u2019s needs.<br\/>\nThey are commonly discussed in acute heart failure, cardiogenic shock, and perioperative cardiac care.<\/p>\n\n\n\n<h2 class=\"wp-block-heading\">Clinical role and significance<\/h2>\n\n\n\n<p>Inotropic Agents matter in cardiology because myocardial contractility is a central determinant of <strong>cardiac output<\/strong> (the amount of blood the heart pumps per minute). When the heart cannot generate enough forward flow\u2014due to <strong>left ventricular (LV) systolic dysfunction<\/strong>, <strong>right ventricular (RV) failure<\/strong>, severe <strong>valvular disease<\/strong>, <strong>myocardial ischemia\/infarction<\/strong>, or decompensated <strong>heart failure<\/strong>\u2014patients can develop hypotension, pulmonary edema, and end-organ hypoperfusion.<\/p>\n\n\n\n<p>Clinically, Inotropic Agents are used to support circulation while clinicians diagnose and treat the underlying problem and optimize loading conditions (preload and afterload). They often sit at the intersection of hemodynamics, pharmacology, and intensive monitoring, and they are frequently paired with therapies such as diuretics, vasopressors, mechanical ventilation, reperfusion strategies in acute coronary syndromes, and <strong>mechanical circulatory support<\/strong> (MCS).<\/p>\n\n\n\n<p>Because these medications can increase myocardial oxygen demand and provoke arrhythmias, their use is typically limited to specific settings where benefits may outweigh risks, and where close monitoring is feasible. Decisions about selection, dosing, and duration vary by clinician and case.<\/p>\n\n\n\n<h2 class=\"wp-block-heading\">Indications \/ use cases<\/h2>\n\n\n\n<p>Typical scenarios where Inotropic Agents may be considered include:<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li><strong>Cardiogenic shock<\/strong> (e.g., after acute myocardial infarction, acute decompensated cardiomyopathy) with low cardiac output and signs of hypoperfusion  <\/li>\n<li><strong>Acute decompensated heart failure<\/strong> with reduced ejection fraction (HFrEF) and low-output features (cold extremities, low urine output, altered mentation), especially when hypotension limits other therapies  <\/li>\n<li><strong>Post\u2013cardiac surgery<\/strong> low cardiac output syndrome (post-cardiotomy myocardial dysfunction)  <\/li>\n<li><strong>RV failure<\/strong> (including RV infarction, pulmonary hypertension\u2013related RV decompensation) where contractility support may improve forward flow  <\/li>\n<li><strong>Bridge therapy<\/strong> in advanced heart failure (e.g., bridge to transplant evaluation, bridge to durable LVAD in selected cases)  <\/li>\n<li><strong>Stress testing contexts<\/strong> (pharmacologic inotropic stress with dobutamine during echocardiography when exercise testing is not feasible)  <\/li>\n<li>Selected <strong>bradyarrhythmia-related low output<\/strong> states where chronotropy and inotropy are both needed (varies by clinician and case)<\/li>\n<\/ul>\n\n\n\n<h2 class=\"wp-block-heading\">Contraindications \/ limitations<\/h2>\n\n\n\n<p>There are few absolute contraindications that apply to every agent, but important limitations and \u201cnot ideal\u201d situations include:<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li><strong>Uncorrected hypovolemia<\/strong>: low preload can worsen hypotension and limit response to inotropy  <\/li>\n<li><strong>Ongoing myocardial ischemia<\/strong> or acute coronary syndrome where increased oxygen demand may be undesirable (agent choice and goals vary by clinician and case)  <\/li>\n<li><strong>Significant tachyarrhythmias<\/strong> (e.g., atrial fibrillation with rapid ventricular response, ventricular tachycardia) where some agents can aggravate rate and ectopy  <\/li>\n<li><strong>Severe obstructive physiology<\/strong> such as hypertrophic obstructive cardiomyopathy (HOCM) or dynamic LV outflow tract obstruction, where increased contractility may worsen obstruction  <\/li>\n<li><strong>Marked hypotension with vasodilation<\/strong>: some inodilators can lower systemic vascular resistance (SVR), so a vasopressor-focused strategy may be preferred  <\/li>\n<li><strong>Advanced chronic use<\/strong>: long-term outpatient infusions can be associated with complications (arrhythmias, line infections, progressive heart failure), and appropriateness varies by goals of care and institution  <\/li>\n<li><strong>Limited monitoring capacity<\/strong>: many agents require continuous ECG and frequent blood pressure assessment, often in ICU-level care<\/li>\n<\/ul>\n\n\n\n<h2 class=\"wp-block-heading\">How it works (Mechanism \/ physiology)<\/h2>\n\n\n\n<p><strong>Core physiologic target:<\/strong> Inotropic Agents increase (positive inotropy) or decrease (negative inotropy) the force of myocardial contraction. In cardiology practice, the term usually refers to <strong>positive inotropes<\/strong> used to raise stroke volume and cardiac output.<\/p>\n\n\n\n<h3 class=\"wp-block-heading\">Major mechanisms used clinically<\/h3>\n\n\n\n<ul class=\"wp-block-list\">\n<li>\n<p><strong>\u03b2-adrenergic receptor agonism (catecholamines)<\/strong><br\/>\n  Agents such as <strong>dobutamine<\/strong>, <strong>dopamine<\/strong>, and <strong>epinephrine<\/strong> stimulate \u03b2\u2081 receptors on cardiomyocytes, increasing intracellular cyclic adenosine monophosphate (cAMP). This enhances calcium handling in the sarcoplasmic reticulum, strengthening contraction and often increasing heart rate (chronotropy) and conduction velocity (dromotropy). Depending on receptor selectivity and dose, vascular tone may also change (\u03b1 effects raise SVR; \u03b2\u2082 effects lower SVR).<\/p>\n<\/li>\n<li>\n<p><strong>Phosphodiesterase-3 (PDE3) inhibition (inodilators)<\/strong><br\/>\n<strong>Milrinone<\/strong> prevents cAMP breakdown in cardiac and vascular smooth muscle. This can increase contractility while also causing vasodilation (reduced afterload and sometimes reduced preload). The combined effect may improve forward flow but can also contribute to hypotension in susceptible patients.<\/p>\n<\/li>\n<li>\n<p><strong>Calcium sensitization (where available)<\/strong><br\/>\n<strong>Levosimendan<\/strong> (availability varies by country and institution) increases contractility by sensitizing troponin C to calcium and can also cause vasodilation via potassium-channel effects. Clinical use patterns vary by clinician and case.<\/p>\n<\/li>\n<li>\n<p><strong>Cardiac glycosides (primarily chronic use)<\/strong><br\/>\n<strong>Digoxin<\/strong> increases intracellular calcium indirectly via Na\u207a\/K\u207a-ATPase inhibition and also exerts vagotonic effects that can slow atrioventricular (AV) nodal conduction. Its role is more common in chronic heart failure symptom management and rate control in atrial fibrillation, rather than acute shock resuscitation.<\/p>\n<\/li>\n<\/ul>\n\n\n\n<h3 class=\"wp-block-heading\">Relevant anatomy and hemodynamics<\/h3>\n\n\n\n<ul class=\"wp-block-list\">\n<li><strong>Myocardium (LV and RV):<\/strong> contractility changes primarily affect ventricular ejection and stroke volume.  <\/li>\n<li><strong>Valves:<\/strong> severe aortic stenosis, acute mitral regurgitation, or mechanical complications after infarction can alter the hemodynamic response to inotropy.  <\/li>\n<li><strong>Conduction system:<\/strong> many inotropes increase automaticity and can precipitate atrial or ventricular arrhythmias.  <\/li>\n<li><strong>Coronary arteries:<\/strong> stronger\/faster contraction increases myocardial oxygen consumption; if coronary perfusion is limited, ischemia can worsen.<\/li>\n<\/ul>\n\n\n\n<h3 class=\"wp-block-heading\">Onset, duration, and reversibility<\/h3>\n\n\n\n<p>Most ICU inotropes are given as <strong>continuous intravenous infusions<\/strong> with relatively rapid titratability. Onset and offset vary by drug (and by organ function, particularly renal function for milrinone). Effects are generally <strong>reversible<\/strong> by reducing or stopping the infusion, though downstream consequences (e.g., arrhythmia, ischemia) may persist and require separate management.<\/p>\n\n\n\n<h2 class=\"wp-block-heading\">Inotropic Agents Procedure or application overview<\/h2>\n\n\n\n<p>Inotropic Agents are not a single procedure; they are a medication class applied within a structured hemodynamic workflow.<\/p>\n\n\n\n<ol class=\"wp-block-list\">\n<li>\n<p><strong>Evaluation\/exam<\/strong><br\/>\n   Clinicians assess perfusion (mental status, urine output, skin temperature), congestion (jugular venous pressure, pulmonary edema), blood pressure, and signs of shock.<\/p>\n<\/li>\n<li>\n<p><strong>Diagnostics<\/strong><br\/>\n   Common tools include ECG, chest imaging, laboratory testing (including metabolic markers of hypoperfusion), bedside <strong>echocardiography<\/strong> for ventricular function and valve assessment, and sometimes <strong>right heart catheterization<\/strong> to measure filling pressures and cardiac output.<\/p>\n<\/li>\n<li>\n<p><strong>Preparation<\/strong><br\/>\n   Reversible contributors are addressed (oxygenation\/ventilation, acid\u2013base disturbances, electrolyte abnormalities, preload optimization, and treatment of triggers such as infection or ischemia). Vascular access is established; some agents are ideally administered via central venous access depending on local protocols and concentration.<\/p>\n<\/li>\n<li>\n<p><strong>Intervention\/testing<\/strong><br\/>\n   An inotrope is selected based on the dominant problem (low output vs low SVR, RV vs LV failure, arrhythmia risk, blood pressure profile). The infusion is started and titrated to clinical and hemodynamic targets. In some contexts, inotropy is paired with a vasopressor to maintain perfusion pressure.<\/p>\n<\/li>\n<li>\n<p><strong>Immediate checks<\/strong><br\/>\n   Continuous ECG monitoring, frequent blood pressure assessment, and reassessment for chest pain\/ischemia, arrhythmias, and changes in oxygenation.<\/p>\n<\/li>\n<li>\n<p><strong>Follow-up\/monitoring<\/strong><br\/>\n   Serial reassessment of volume status, renal function, lactate or other perfusion markers (as used locally), and repeat echocardiography when indicated. De-escalation is considered when the underlying condition improves or definitive therapy (revascularization, valve intervention, MCS) is implemented.<\/p>\n<\/li>\n<\/ol>\n\n\n\n<h2 class=\"wp-block-heading\">Types \/ variations<\/h2>\n\n\n\n<p>Inotropic Agents are often grouped by mechanism and by whether they also significantly affect vascular tone.<\/p>\n\n\n\n<h3 class=\"wp-block-heading\">Catecholamine inotropes (\u03b2-agonists; sometimes mixed \u03b1\/\u03b2 effects)<\/h3>\n\n\n\n<ul class=\"wp-block-list\">\n<li><strong>Dobutamine:<\/strong> commonly used for low-output states; can lower SVR slightly due to \u03b2\u2082 activity in some patients.  <\/li>\n<li><strong>Dopamine:<\/strong> dose-dependent receptor profile; may increase heart rate and arrhythmia risk; its use varies by institution and guideline interpretation.  <\/li>\n<li><strong>Epinephrine:<\/strong> strong \u03b2 and \u03b1 effects; can increase contractility and SVR; often used in profound shock but may raise lactate via metabolic effects (interpretation varies by clinician and case).  <\/li>\n<li><strong>Isoproterenol:<\/strong> potent \u03b2 agonist with marked chronotropy; used selectively (e.g., certain bradyarrhythmias) rather than routine cardiogenic shock.<\/li>\n<\/ul>\n\n\n\n<h3 class=\"wp-block-heading\">Inodilators (increase contractility and reduce afterload)<\/h3>\n\n\n\n<ul class=\"wp-block-list\">\n<li><strong>Milrinone (PDE3 inhibitor):<\/strong> useful when \u03b2-receptor downregulation or beta-blockade is a concern; vasodilation can limit use in hypotension. Renal clearance makes dosing\/accumulation considerations important.  <\/li>\n<li><strong>Levosimendan (calcium sensitizer; where available):<\/strong> longer-acting metabolites may extend hemodynamic effects beyond the infusion; clinical adoption varies by region.<\/li>\n<\/ul>\n\n\n\n<h3 class=\"wp-block-heading\">\u201cInotropy in broader hemodynamic support\u201d<\/h3>\n\n\n\n<ul class=\"wp-block-list\">\n<li><strong>Norepinephrine<\/strong> is primarily a vasopressor (\u03b1 effect) but has some \u03b2\u2081 activity; it is often paired with an inotrope in mixed shock states.  <\/li>\n<li><strong>Vasopressin<\/strong> is not an inotrope; it raises SVR through non-adrenergic mechanisms and may be used as an adjunct in vasodilatory shock.<\/li>\n<\/ul>\n\n\n\n<h3 class=\"wp-block-heading\">Chronic\/adjunct positive inotropy<\/h3>\n\n\n\n<ul class=\"wp-block-list\">\n<li><strong>Digoxin:<\/strong> oral agent with slower onset and narrower therapeutic window; typically not a first-line drug for acute hemodynamic collapse.<\/li>\n<\/ul>\n\n\n\n<h2 class=\"wp-block-heading\">Advantages and limitations<\/h2>\n\n\n\n<p>Advantages:<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Supports <strong>cardiac output<\/strong> in low-flow states when perfusion is threatened  <\/li>\n<li>Can be <strong>titrated<\/strong> relatively quickly in monitored settings (especially IV infusions)  <\/li>\n<li>Useful as a <strong>bridge<\/strong> while definitive therapy is pursued (revascularization, valve intervention, MCS, transplant evaluation)  <\/li>\n<li>May improve symptoms related to low output (fatigue, cool extremities) in selected settings  <\/li>\n<li>Inodilators can reduce <strong>afterload<\/strong>, which may benefit some patients with LV failure  <\/li>\n<li>Can provide controlled <strong>pharmacologic stress<\/strong> in dobutamine stress echocardiography<\/li>\n<\/ul>\n\n\n\n<p>Limitations:<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Can provoke <strong>tachyarrhythmias<\/strong> and increase myocardial irritability  <\/li>\n<li>May increase <strong>myocardial oxygen demand<\/strong>, potentially worsening ischemia in susceptible patients  <\/li>\n<li>Hypotension can occur, particularly with agents that vasodilate  <\/li>\n<li>Requires close monitoring (ECG, blood pressure, end-organ function), often ICU-level care  <\/li>\n<li>Response is highly <strong>context-dependent<\/strong> (preload, afterload, RV vs LV failure, valve disease)  <\/li>\n<li>Prolonged reliance may signal advanced disease; long-term infusion strategies carry risks and are individualized<\/li>\n<\/ul>\n\n\n\n<h2 class=\"wp-block-heading\">Follow-up, monitoring, and outcomes<\/h2>\n\n\n\n<p>Monitoring during and after Inotropic Agents therapy focuses on whether perfusion and congestion are improving without unacceptable adverse effects. Outcomes are influenced by the <strong>underlying diagnosis<\/strong> (e.g., reversible ischemia vs progressive cardiomyopathy), baseline ventricular function, comorbidities (chronic kidney disease, pulmonary hypertension), and the degree of shock or hypoperfusion at presentation.<\/p>\n\n\n\n<p>Common monitoring domains include:<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li><strong>Hemodynamics:<\/strong> blood pressure, heart rate, signs of adequate perfusion, and (when used) invasive measures such as central venous pressure or pulmonary artery catheter data  <\/li>\n<li><strong>Rhythm surveillance:<\/strong> continuous ECG for atrial fibrillation with rapid ventricular response, ventricular ectopy, or sustained ventricular arrhythmias  <\/li>\n<li><strong>End-organ function:<\/strong> urine output, kidney function trends, mental status, and other organ-specific markers used locally  <\/li>\n<li><strong>Congestion status:<\/strong> pulmonary edema on exam or imaging, oxygen requirements, and volume status assessments  <\/li>\n<li><strong>Therapy trajectory:<\/strong> whether the inotrope can be weaned as diuresis, reperfusion, afterload reduction, or mechanical support is optimized<\/li>\n<\/ul>\n\n\n\n<p>In advanced heart failure, clinicians may also assess candidacy for device therapy (e.g., implantable cardioverter-defibrillator [ICD], cardiac resynchronization therapy [CRT]) and MCS (IABP, Impella, VA-ECMO, durable LVAD), but the timing and selection vary by institution and patient goals.<\/p>\n\n\n\n<h2 class=\"wp-block-heading\">Alternatives \/ comparisons<\/h2>\n\n\n\n<p>Management of low cardiac output and shock is rarely \u201cinotrope vs no inotrope\u201d; it is usually a layered strategy. Common alternatives or complements include:<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li><strong>Observation\/monitoring and treating the trigger:<\/strong> Some patients improve with oxygen, diuretics, rhythm control, reperfusion, or correction of precipitating factors without requiring inotropy.  <\/li>\n<li><strong>Vasopressors (perfusion pressure strategy):<\/strong> In vasodilatory or mixed shock, raising SVR with norepinephrine (or other agents) may be prioritized, with inotropy added if cardiac output remains inadequate.  <\/li>\n<li><strong>Afterload reduction without inotropy:<\/strong> In selected heart failure presentations with adequate blood pressure, vasodilators can improve forward flow by decreasing afterload, potentially reducing the need for inotropes (varies by clinician and case).  <\/li>\n<li><strong>Mechanical circulatory support:<\/strong> IABP, percutaneous ventricular assist devices, VA-ECMO, or durable LVAD can provide more substantial circulatory support when medications are insufficient or poorly tolerated. Device choice depends on anatomy, RV involvement, respiratory status, and institutional resources.  <\/li>\n<li><strong>Definitive procedural therapy:<\/strong> Revascularization for acute coronary occlusion, valve repair\/replacement for acute severe valvular lesions, or treatment of mechanical complications of myocardial infarction may address the cause rather than relying on pharmacologic support.  <\/li>\n<li><strong>Palliative-focused care:<\/strong> In advanced, refractory disease, goals-of-care\u2013aligned symptom management may be emphasized; approaches vary by clinician and case.<\/li>\n<\/ul>\n\n\n\n<h2 class=\"wp-block-heading\">Inotropic Agents Common questions (FAQ)<\/h2>\n\n\n\n<p><strong>Q: Are Inotropic Agents the same as vasopressors?<\/strong><br\/>\nNo. Inotropic Agents primarily increase the force of cardiac contraction, while vasopressors primarily increase vascular tone to raise blood pressure. Some drugs have mixed effects, so clinicians choose based on whether the dominant problem is low cardiac output, low SVR, or both.<\/p>\n\n\n\n<p><strong>Q: Do Inotropic Agents cause pain or discomfort?<\/strong><br\/>\nThe medications themselves do not typically cause pain, but they are often given by IV infusion in monitored settings, which can involve discomfort from IV lines or frequent blood pressure checks. Symptoms like palpitations or tremor can occur with some agents due to adrenergic stimulation.<\/p>\n\n\n\n<p><strong>Q: Do patients need anesthesia to receive Inotropic Agents?<\/strong><br\/>\nNo anesthesia is required to administer an inotrope infusion. However, inotropes are often used in ICU care where other procedures (intubation, central line placement, cardiac catheterization, surgery) may involve sedation or anesthesia depending on the situation.<\/p>\n\n\n\n<p><strong>Q: How long do the effects of Inotropic Agents last?<\/strong><br\/>\nMany IV inotropes begin working quickly and can be adjusted minute-to-minute, with effects diminishing after the infusion is reduced or stopped. Duration varies by drug and patient factors such as kidney function and overall perfusion.<\/p>\n\n\n\n<p><strong>Q: Are Inotropic Agents \u201csafe\u201d?<\/strong><br\/>\nThey can be appropriate and beneficial in selected clinical scenarios, but they carry meaningful risks, including arrhythmias, ischemia, and blood pressure instability. Safety depends on the agent, dose, monitoring intensity, and the underlying cardiac condition.<\/p>\n\n\n\n<p><strong>Q: How are patients monitored while on Inotropic Agents?<\/strong><br\/>\nMonitoring commonly includes continuous ECG, frequent blood pressure assessment, and reassessment of urine output and organ function. Some patients require invasive hemodynamic monitoring or repeat echocardiography, depending on severity and diagnostic uncertainty.<\/p>\n\n\n\n<p><strong>Q: Do Inotropic Agents replace standard heart failure medications?<\/strong><br\/>\nNot usually. Guideline-directed medical therapy for chronic heart failure (such as beta-blockers, renin\u2013angiotensin system inhibitors, mineralocorticoid receptor antagonists, and SGLT2 inhibitors) targets long-term remodeling and outcomes, whereas inotropes are typically short-term support for acute low-output states. How therapies are balanced varies by clinician and case.<\/p>\n\n\n\n<p><strong>Q: Will activity be restricted after receiving Inotropic Agents?<\/strong><br\/>\nActivity recommendations depend on the underlying illness (e.g., cardiogenic shock, postoperative recovery) rather than the medication alone. Many patients receiving inotropes are acutely ill and are managed in monitored settings where mobility is guided by clinical stability and staffing protocols.<\/p>\n\n\n\n<p><strong>Q: What is the typical recovery expectation after needing Inotropic Agents?<\/strong><br\/>\nRecovery depends on the cause of low output\u2014such as reversible ischemia, myocarditis, decompensated chronic heart failure, or postoperative stunning\u2014and on how quickly the cause is corrected. Some patients can be weaned as hemodynamics improve, while others may require escalation to device therapy or longer-term planning; this varies by clinician and case.<\/p>\n\n\n\n<p><strong>Q: What do Inotropic Agents cost?<\/strong><br\/>\nCosts vary widely by medication, duration of infusion, monitoring requirements, and care setting (ICU vs step-down vs procedural lab). Institutional formulary choices and regional pricing also affect total cost of care.<\/p>\n\n\n\n<p><strong>Q: How often are follow-up checks needed after inotrope therapy?<\/strong><br\/>\nFollow-up depends on the severity of the episode and the underlying diagnosis. Many patients need reassessment of volume status, renal function, rhythm, and ventricular function after stabilization, with the interval tailored to inpatient course and discharge planning.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Inotropic Agents are medications that change the force of heart muscle contraction. They are a therapy used in cardiovascular and critical care medicine. They are most often used when cardiac output is inadequate for the body\u2019s needs. They are commonly discussed in acute heart failure, cardiogenic shock, and perioperative cardiac care.<\/p>\n","protected":false},"author":10,"featured_media":0,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[],"tags":[],"class_list":["post-2653","post","type-post","status-publish","format-standard","hentry"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v25.7 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>Inotropic Agents: Definition, Clinical Significance, and Overview - Best Heart Surgery Hospitals<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/www.bestheartsurgery.com\/blog\/inotropic-agents-definition-clinical-significance-and-overview\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Inotropic Agents: Definition, Clinical Significance, and Overview - Best Heart Surgery Hospitals\" \/>\n<meta property=\"og:description\" content=\"Inotropic Agents are medications that change the force of heart muscle contraction. 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